Abstract:Context:
Guidelines has systematically suggested genetic testing for a wide spectrum of phenotypes in order to confirm or exclude surely the diagnosis of multiple endocrine neoplasia type 1 (MEN1). However, the probability of find a germline
MEN1
mutation has showed extremely variable (5-95%) when different phenotypes are considered. The prompt recognition of potential clinical predictors could anticipate the result of the genetic testing in the different clinical scenarios.
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